3D genome organization links non-coding disease-associated variants to genes
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DOI: 10.3389/fcell.2022.995388
Abstract: Genome sequencing has revealed over 300 million genetic variations in human populations. Over 90% of variants are single nucleotide polymorphisms (SNPs), the remainder include short deletions or insertions, and small numbers of structural variants. Hundreds… read more here.
Keywords: coding disease; associated snps; gene; disease associated ... See more keywords